Drug Information
Drug General Information | Top | |||
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Drug ID |
D0SZ9F
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Former ID |
DNC011149
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Drug Name |
2,4-Dichlorobenzenemethanethiol
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Synonyms |
2,4-Dichlorobenzyl mercaptan; 59293-67-3; (2,4-Dichlorophenyl)methanethiol; 2,4-Dichlorobenzylmercaptan; 2,4-dichlorophenylmethanethiol; 2,4-Dichlorobenzenemethanethiol; 2,4-Dichloro-alpha-toluenethiol; 2,4-Dichlorotoluene-alpha-thiol; Benzenemethanethiol, 2,4-dichloro-; CHEMBL1224561; ZSPXTTVUJDSRNJ-UHFFFAOYSA-N; NSC33218; EINECS 261-687-2; AI3-31458; AC1Q3MDQ; ACMC-1B9KZ; AC1L3V0Z; SCHEMBL1802752; 2,4-Dichlorothiobenzyl Alcohol; ZSPXTTVUJDSRNJ-UHFFFAOYSA-; CTK5A9733; DTXSID70208016; MolPort-004-354-551
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Drug Type |
Small molecular drug
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Indication | Discovery agent [ICD-11: N.A.] | Investigative | [1] | |
Structure |
Download2D MOL |
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Formula |
C7H6Cl2S
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Canonical SMILES |
C1=CC(=C(C=C1Cl)Cl)CS
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InChI |
1S/C7H6Cl2S/c8-6-2-1-5(4-10)7(9)3-6/h1-3,10H,4H2
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InChIKey |
ZSPXTTVUJDSRNJ-UHFFFAOYSA-N
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CAS Number |
CAS 59293-67-3
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PubChem Compound ID |
Target and Pathway | Top | |||
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Target(s) | Indoleamine 2,3-dioxygenase 1 (IDO1) | Target Info | Inhibitor | [1] |
BioCyc | Superpathway of tryptophan utilization | |||
Tryptophan degradation | ||||
L-kynurenine degradation | ||||
Tryptophan degradation to 2-amino-3-carboxymuconate semialdehyde | ||||
NAD de novo biosynthesis | ||||
KEGG Pathway | Tryptophan metabolism | |||
Metabolic pathways | ||||
African trypanosomiasis | ||||
NetPath Pathway | TSLP Signaling Pathway | |||
IL5 Signaling Pathway | ||||
TGF_beta_Receptor Signaling Pathway | ||||
Pathwhiz Pathway | Tryptophan Metabolism | |||
Reactome | Tryptophan catabolism | |||
WikiPathways | Tryptophan metabolism | |||
Metabolism of amino acids and derivatives |
References | Top | |||
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REF 1 | S-benzylisothiourea derivatives as small-molecule inhibitors of indoleamine-2,3-dioxygenase. Bioorg Med Chem Lett. 2010 Sep 1;20(17):5126-9. |
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